1,3-Dimethyl-2-imidazolidinone → 4-Bromo-2-fluoro-1-(pentafluoroethyl)benzene

온도

0 °C

13.2 g (91.9 mmol) of copper(I) bromide were cooled to −5° C. in 80 ml of dry N,N-dimethylformamide. Under nitrogen, 14.7 g (76.7 mmol) of trimethyl-(pentafluoroethyl)silane were added. 4.45 g (76.7 mmol) of potassium fluoride (spray-dried) were added in portions over the course of 30 minutes at a rate such that the internal temperature remained below 0° C. The mixture was stirred at 0° C. for 1 hour and was then warmed to 20° C. over the course of 12 hours. Thereafter 10 ml of dry 1,3-dimethyl-2-imidazolidinone and 22 g (73.1 mmol) of 3-fluoro-4-iodo-bromobenzene were added. The contents were stirred at 75° C. for 14 hours. Then all of the volatile constituents were distilled off to dryness, the distillate being collected in a cold trap cooled with liquid nitrogen. The distillate was subsequently warmed to 20° C. and dissolved in 500 ml of diethyl ether. This solution was washed with four times 100 ml of water and then with two times 100 ml of saturated aqueous NaCl solution. The organic phase was then dried, and the solvent was removed on a Vigreux column. Subsequent distillation of the residue on a Vigreux column gave 16.1 g of product (boiling point: 86-87° C. (75 mmHg)) with a purity of 99% by weight.

1. customremained below 0° C
2. temperaturewas then warmed to 20° C. over the course of 12 hours
3. stirringThe contents were stirred at 75° C. for 14 hours
4. distillationThen all of the volatile constituents were distilled off to dryness
5. distillationthe distillate being collected in a cold trap
6. temperaturecooled with liquid nitrogen
7. temperatureThe distillate was subsequently warmed to 20° C.
8. dissolutiondissolved in 500 ml of diethyl ether
9. washThis solution was washed with four times 100 ml of water
10. customThe organic phase was then dried
11. customthe solvent was removed on a Vigreux column
12. distillationSubsequent distillation of the residue on a Vigreux column

ORD 기록

ord-faefb4c7c7d94a77a0244a50fc1c464e

출처 데이터셋

uspto-grants-2013_09

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US08536097B2